Quality Control Technician

Quality Control TechnicianPay Range: $25/hr to $27/hrLocation: Scarborough, ME 04074Work Type: OnsiteContract Duration: 6 Months, Possible ExtensionJob Summary:The Quality Control Technician will support laboratory testing and quality control operations within a regulated medical device manufacturing environment. This role is responsible for performing in process and final release testing of Lateral Flow, ELISA, and Molecular products. The individual will ensure product quality and compliance with established quality systems and applicable regulatory requirements. The position requires hands on laboratory experience, strong attention to detail, and the ability to accurately document testing results. The ideal candidate will have experience with laboratory equipment, troubleshooting, and Good Manufacturing and Laboratory Practices.Key Responsibilities:Perform in process testing of components used in Lateral Flow, ELISA, and Molecular products.Conduct final release testing to ensure products meet established quality standards and specifications.Troubleshoot technical and quality related issues encountered during laboratory testing.Perform laboratory procedures using appropriate equipment while following established safety precautions.Review batch records and verify the accuracy and completeness of quality documentation.Calibrate, maintain, and operate laboratory equipment according to established procedures.Follow Good Manufacturing Practices and Good Laboratory Practices to maintain regulatory compliance.Accurately document laboratory test results and report any deviations from approved procedures.Support Quality Management System activities and contribute to continuous quality improvement.Maintain laboratory cleanliness and perform cleaning activities using approved cleaning agents.Required Qualifications:Associate degree in Biology, Chemistry, Life Sciences, or another related technical field, or an equivalent combination of education and experience.At least 1 year of laboratory and or Quality Control experience.Ability to follow established GMP and GLP procedures.Ability to accurately document laboratory testing results and follow technical procedures.Strong attention to detail and ability to identify deviations from approved manufacturing procedures.Basic computer proficiency, including database, inventory, spreadsheet, and word processing applications.Ability to read, interpret, and follow technical documents, safety guidelines, and standard operating procedures.Preferred Qualifications:Bachelor's degree in a scientific or technical discipline.At least 2 years of experience in a regulated industry.At least 2 years of experience with GMP, FDA, ISO, or USDA regulations.Previous experience in a Quality Assurance or Quality Control role within the medical device industry.Hands on experience with pipettes, pH meters, and ELISA assays.Knowledge of enzyme based and immunochromatographic assays.Experience with inspection systems, systematic troubleshooting, statistics, and data analysis.Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable